GMP, WHO-GMP & ISO
Certified Manufacturing
You Can Verify
Every facility under the Jireh Nutrition Hub network is independently audited, certified, and maintained to the highest international manufacturing standards — not because regulations require it, but because the brands we serve in the USA, UK, Europe, and UAE demand nothing less. Here is the complete picture of our compliance infrastructure.
Certifications Are Not
a Checkbox. They Are
Your Brand’s Insurance.
For any supplement or pharmaceutical brand selling in the United States, United Kingdom, European Union, or the Gulf, the question of manufacturer certification is not procedural — it is existential. A single regulatory violation, a failed customs inspection, or a product recall traced to a non-compliant manufacturer can destroy years of brand equity overnight.
At Jireh Nutrition Hub, we do not treat certifications as marketing assets. They are the operational backbone of everything we manufacture. Every certificate you see on this page was earned through independent third-party audits — not claimed through self-assessment — and every one is actively maintained across audit cycles.
When you source from a Jireh-certified facility, you are not just buying manufacturing capacity. You are buying the compliance infrastructure that protects your brand from the moment your product leaves India to the moment it reaches the end consumer.
Every Certificate.
Every Facility.
Fully Documented.
Below is a complete breakdown of every active certification held across the Jireh Nutrition Hub manufacturing network — what each standard requires, what it means for your products, and which categories of manufacturing it covers.
Good Manufacturing Practice is the global baseline standard for pharmaceutical and supplement manufacturing. GMP certification means our facilities meet strict requirements across personnel, premises, equipment, raw material sourcing, production processes, quality control, packaging, labelling, and distribution. Every Jireh Nutrition Hub facility is GMP-certified and independently audited on a recurring cycle. GMP is the non-negotiable prerequisite for any product we manufacture — without it, we don’t produce a single unit.
WHO-GMP is the internationally recognised pharmaceutical manufacturing standard issued by the World Health Organization — and the primary compliance credential required by regulatory authorities in over 100 countries for pharmaceutical product import and registration. Our WHO-GMP certification means our pharmaceutical manufacturing units meet the full technical requirements of WHO TRS 823, Annex 1 — covering everything from cleanroom environments and sterile manufacturing through to batch documentation, recall procedures, and stability testing protocols. For brands selling pharmaceutical or nutraceutical products in regulated markets, WHO-GMP is the document that opens doors.
ISO 9001:2015 is the world’s most recognised Quality Management System standard. Unlike product-specific certifications, ISO 9001 certifies the entire organisation’s process discipline — from how we handle client enquiries and specification agreements, through to production planning, in-process monitoring, non-conformance management, corrective action protocols, and continuous improvement cycles. Our ISO 9001:2015 certification validates that the quality outcomes we deliver are not the result of individual effort but of a repeatable, audited, system-driven approach. For international clients, this translates to one clear guarantee: every batch we produce is made the same way, to the same standard, every time.
The FSSAI Central License is India’s highest-tier food manufacturing authorisation, issued under the Food Safety and Standards Act, 2006. It is a mandatory legal requirement for any food supplement or nutraceutical manufacturer operating above defined production thresholds in India — and it is the foundational document required by Indian customs for export of any food, supplement, or Ayurvedic product. Our FSSAI Central License covers the full range of nutraceutical, functional food, Ayurvedic supplement, and herbal product categories we manufacture, and is renewed annually through ongoing compliance audits conducted by the Food Safety Commissioner’s office.
HACCP is the internationally mandated food safety management system that identifies, evaluates, and controls biological, chemical, and physical hazards at every critical point in the manufacturing process — from raw material intake through to finished product dispatch. Our HACCP certification means we have formally mapped every stage of production, identified every point at which contamination or quality deviation could occur, and established verified control measures at each critical control point. For supplement brands selling into US, EU, and Australian markets — where food safety due diligence is increasingly enforced at the retail and platform level — HACCP documentation from your manufacturer is rapidly becoming a commercial prerequisite.
Our nutraceutical and dietary supplement manufacturing facilities operate in full compliance with FDA 21 CFR Part 111 — the US federal regulation governing Current Good Manufacturing Practice for dietary supplements. This means our facilities meet the documentation, identity testing, purity verification, batch traceability, and qualified person requirements that FDA inspectors look for when auditing foreign supplement manufacturers. While the FDA does not issue a formal “certification” to overseas facilities, compliance with 21 CFR Part 111 is verifiable through our internal SOPs, batch manufacturing records, and third-party audit reports — all of which we make available to US brand clients on request.
Our USDA Organic certification covers the production of certified organic botanical extracts, herbal powders, and nutraceutical ingredients for brands selling into the United States organic supplement market. USDA Organic is one of the most stringent agricultural and processing certifications in the world — requiring complete pesticide-free cultivation, non-GMO sourcing, segregated organic processing lines, and full traceability from farm to finished product. Our certified organic ingredient range includes Ashwagandha, Moringa, Turmeric, Tulsi, Amla, Triphala, and 30+ additional botanicals — all available for incorporation into your certified organic private label product.
APEDA registration is the mandatory Government of India export licence for agricultural products, processed food items, herbal and Ayurvedic preparations, and organic products leaving Indian borders. As a registered APEDA exporter, Jireh Nutrition Hub is authorised to issue the Phytosanitary Certificates and APEDA-endorsed documentation required by destination country customs authorities worldwide — particularly for plant-origin botanical ingredients and Ayurvedic products. APEDA registration is not available to unregistered manufacturers and is a prerequisite for any legitimate botanical ingredient export from India.
Our Certifications
Open Every Major
Global Market
Each international market has its own regulatory gatekeepers. Our certification portfolio is deliberately structured to satisfy the requirements of every major supplement and pharmaceutical import authority simultaneously — so your product doesn’t just get manufactured, it gets cleared.
The US supplement market operates under 21 CFR Part 111 GMP requirements enforced by the FDA. Our compliant infrastructure and documentation stack fully satisfies US Customs, Amazon’s supplement compliance requirements, and major US retailer sourcing policies.
Post-Brexit, the UK operates an independent regulatory framework under the MHRA and Food Standards Agency. Our documentation package covers UKCA-aligned manufacturing evidence, EC-equivalent CoAs, and Certificate of Origin for UK customs processing.
EU supplement imports are governed by the European Food Safety Authority and EU Novel Food Regulation EC 2015/2283. Our GMP and ISO 9001 certifications satisfy EU manufacturing evidence requirements, and we provide full EFSA-referenced safety documentation for applicable botanicals.
The UAE and GCC supplement market requires Halal certification, WHO-GMP alignment, and ESMA-compliant labelling for product registration. Our WHO-GMP certification and Halal documentation package makes product registration with Dubai Health Authority and Saudi SFDA straightforward.
Australia’s Therapeutic Goods Administration operates one of the world’s most rigorous supplement import frameworks. TGA registration requires evidence of GMP-compliant overseas manufacturing. Our certification documentation is formatted to meet TGA overseas GMP clearance requirements for complementary medicine manufacturers.
Singapore’s HSA, Indonesia’s BPOM, Nigeria’s NAFDAC, and other Asia-Pacific and African regulators accept WHO-GMP certification as the primary overseas manufacturing standard. Our WHO-GMP documentation and Free Sale Certificates have been accepted across 12+ APAC and African jurisdictions.
The Quality Infrastructure
That Earns These
Certifications
A certification is only as good as the quality systems behind it. Here is a transparent look at the testing methods, laboratory equipment, and in-process controls that our auditors verify — and that your product depends on.
Jireh vs. The
Typical Indian
Manufacturer
Not every Indian manufacturer is equal — and not every certificate is worth the paper it is printed on. Here is an honest comparison of what Jireh Nutrition Hub’s compliance infrastructure delivers versus the standard you will find at a typical Indian contract manufacturer operating without international market focus.
| Compliance Standard | Jireh Nutrition Hub | Typical Indian Manufacturer | US / EU Manufacturer |
|---|---|---|---|
| GMP Certification | ✓ All 4 facilities | ◑ Some facilities | ✓ Standard |
| WHO-GMP | ✓ Pharma units | ✗ Rarely held | ◑ Varies |
| ISO 9001:2015 | ✓ Full organisation | ✗ Uncommon | ✓ Standard |
| HACCP | ✓ All food categories | ✗ Rarely held | ✓ Standard |
| US FDA 21 CFR Part 111 Compliance | ✓ Fully aligned | ✗ Rarely documented | ✓ Mandatory |
| USDA Organic Certification | ✓ Organic range | ✗ Almost never | ◑ Select facilities |
| Third-Party Lab Reports (NABL) | ✓ Available per batch | ◑ Sporadic | ✓ Standard |
| Complete Export Documentation | ✓ All markets covered | ◑ Basic CoA only | ✓ Standard |
| Manufacturing Cost vs. Quality | ✓ 40–60% below US/EU | ◑ Low cost, lower quality | ✗ Full premium pricing |
Every Document
Your Regulatory
Team Needs
Regulatory submissions, customs clearances, retailer audits, Amazon compliance checks — every one of them requires specific documents from your manufacturer. We have them all, formatted for your destination market, and ready to dispatch alongside your shipment or in advance of your product launch.
We Welcome
Audits. Announced or Not.
Questions International
Buyers Ask About Our Compliance
Need Our Compliance
Documents for Your
Regulatory Team?
We issue GMP certificates, WHO-GMP documents, CoA samples, and our full compliance documentation pack to prospective clients within 24 hours. No commitment required. If your regulatory team or sourcing manager needs to verify our credentials before your enquiry moves forward — this is where you start.